| Primary Device ID | 03600040995259 |
| NIH Device Record Key | 5d455666-9345-4043-bf17-e54b8c2b5ac6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ReTrace |
| Version Model Number | ALXL12 |
| Catalog Number | ALXL12 |
| Company DUNS | 305524696 |
| Company Name | Coloplast A/S |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com | |
| Phone | +1(800)258-3476 |
| urology@coloplast.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03600040995242 [Primary] |
| GS1 | 03600040995259 [Package] Contains: 03600040995242 Package: Retail Box [1 Units] In Commercial Distribution |
| GS1 | 03600040995266 [Package] Package: Shipper Box [24 Units] In Commercial Distribution |
| FED | endoscopic access overtube, gastroenterology-urology |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-28 |
| Device Publish Date | 2024-11-20 |
| 03600040995389 | AXXL12 |
| 03600040995341 | AXXL10 |
| 03600040995310 | ASXL12 |
| 03600040995280 | ASXL10 |
| 03600040995259 | ALXL12 |
| 03600040995235 | ALXL10 |
| 03600040995198 | ACXL12 |
| 03600040995167 | ACXL10 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() RETRACE 97605031 not registered Live/Pending |
Graf Research Corporation 2022-09-23 |
![]() RETRACE 90290340 not registered Live/Pending |
Impressive Sales Inc. 2020-10-30 |
![]() RETRACE 88515345 not registered Live/Pending |
Code Walker, LLC 2019-07-15 |
![]() RETRACE 88514229 not registered Live/Pending |
Columbia Insurance Company 2019-07-15 |
![]() RETRACE 85181617 4231605 Dead/Cancelled |
Celestron Acquisition, LLC 2010-11-19 |
![]() RETRACE 79333352 not registered Live/Pending |
Retrace Group Limited 2021-05-18 |
![]() RETRACE 79081987 3924912 Live/Registered |
Coloplast A/S 2010-03-10 |
![]() RETRACE 74522331 1986096 Dead/Cancelled |
DeRoyal Industries, Inc. 1994-05-04 |